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Contrast-Enhanced Endoscopic Ultrasound Detects Early Therapy Response Following Anti-TNF Therapy in Patients with Ulcerative Colitis

Mark Ellrichmann, Berenice Schulte, Claudio C Conrad, Stephan Schoch, Johannes Bethge, Marcus Seeger, Robert Huber, Madita Goeb, Alexander Arlt, Susanna Nikolaus, Christoph Röcken, Stefan Schreiber

Abstract

Though colonoscopy plays a crucial role in assessing active ulcerative colitis [aUC], its scope is limited to the mucosal surface. Endoscopic ultrasound [EUS] coupled with contrast-enhancement [dCEUS] can precisely quantify bowel wall thickness and microvascular circulation, potentially enabling the quantitative evaluation of inflammation. We conducted a prospective, longitudinal study to assess therapy response using dCEUS in aUC patients undergoing treatment with adalimumab [ADA] or infliximab [IFX].Thirty ADA- and 15 IFX-treated aUC patients were examined at baseline and at 2, 6, and 14 weeks of therapy and 48 weeks of follow-up. Bowel wall thickness [BWT] was measured by EUS in the rectum. Vascularity was quantified by dCEUS using rise time [RT] and time to peak [TTP]. Therapy response was defined after 14 weeks using the Mayo Score.Patients with aUC displayed a mean BWT of 3.9 ± 0.9 mm. In case of response to ADA/IFX a significant reduction in BWT was observed after 2 weeks [p = 0.04], whereas non-responders displayed no significant changes. The TTP was notably accelerated at baseline and significantly normalized by week 2 in responders [p = 0.001], while non-responders exhibited no significant alterations [p = 0.9]. At week 2, the endoscopic Mayo score did not exhibit any changes, thus failing to predict treatment responses.dCEUS enables the early detection of therapy response in patients with aUC, which serves as a predictive marker for long-term clinical success. Therefore, dCEUS serves as a diagnostic tool for assessing the probability of future therapy success.
OriginalspracheEnglisch
ZeitschriftJournal of Crohn's and Colitis
Jahrgang18
Ausgabenummer7
Seiten (von - bis)1012-1024
Seitenumfang13
ISSN1873-9946
DOIs
PublikationsstatusVeröffentlicht - 06.08.2024

Fördermittel

M. Ellrichmann and J. Bethge received travel grants from Abbvie. S. Nikolaus received consulting/lecture fees from Janssen and AbbVie. S. Schreiber received consulting fees from Abbvie [Ludwigshafen, Germany], Amgen [Munich, Germany], Celltrion [Seoul, Korea], Janssen [Neuss, Germany], MSD [Haar, Germany], Pfizer [New York, USA], Sandoz [N\u00FCrnberg, Germany], and Takeda [Berlin, Germany]. B. Schulte, Claudio C. Conrad, Stephan Schoch, Markus Seeger, Robert Huber, Madita Goeb, Alexander Arlt, and Christoph Roecken have no financial conflicts of interest. No commercial entities had any influence on or information about the study design, data collection, data analysis, or writing of the manuscript that could potentially affect the outcome of the study. Acknowledgments This work was supported by the German Research Foundation [grant number EXC 2167-390884018] as well as internal funding by the Department of Interdisciplinary Endoscopy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.

TrägerTrägernummer
AbbVie Deutschland
Schleswig-Holstein
German-Russian Interdisciplinary Science Center
German Israeli Foundation for Scientific Research and DevelopmentEXC 2167-390884018
German Israeli Foundation for Scientific Research and Development

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    Strategische Forschungsbereiche und Zentren

    • Forschungsschwerpunkt: Biomedizintechnik

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    • 2.22-32 Medizinische Physik, Biomedizinische Technik

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